Canonical Allele Identifier: CA491151466
Gene: HCN4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.73621947G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73329606G>C , CM000677.2:g.73329606G>C GRCh38
NC_000015.9:g.73621947G>C , CM000677.1:g.73621947G>C GRCh37
NC_000015.8:g.71409000G>C NCBI36
NG_009063.1:g.44659C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.1557C>G MANE Select ENSP00000261917.3:p.Ser519=
ENST00000261917.3:c.1557C>G ENSP00000261917.3:p.Ser519=
NM_005477.2:c.1557C>G NP_005468.1:p.Ser519=
XM_011521148.1:c.339C>G XP_011519450.1:p.Ser113=
XM_011521148.2:c.339C>G XP_011519450.1:p.Ser113=
NM_005477.3:c.1557C>G MANE Select NP_005468.1:p.Ser519=